Variation of urinary excretion of aspartylglucosamine and associated clinical findings in aspartylglucosaminuria
- 1 December 1980
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 3 (1) , 159-161
- https://doi.org/10.1007/bf02312551
Abstract
The urinary excretion of aspartylglucosamine (AADG), the main accumulating glycoprotein degradation product in aspartylglucosaminuria (AGU), was studied in 40 patients at various stages of the disease. Only slight variation was found when the amount of AADG excreted by ten AGU patients under 10 years of age was compared with AADG excretion of older patients at a clinically advanced stage of the disease. The 24 h AADG excretion of the younger patients was 354 mg compared with 441 mg in the group often patients over 20 years of age. Clinical symptoms were unrelated to AADG excretion.Keywords
This publication has 16 references indexed in Scilit:
- Characterization of the Storage Material of Peripheral Lymphocytes in AspartylglycosaminuriaClinical Science, 1980
- Use of triphenylmethane as an indicator of complete methylation of glycolipids and glycopeptidesCarbohydrate Research, 1979
- Identification of in biological materials by gas chromatography-mass spectrometryClinica Chimica Acta; International Journal of Clinical Chemistry, 1979
- Aspartylglycosaminuria in Northern Norway in eight patients: Clinical heterogeneity and variations with the dietJournal of Inherited Metabolic Disease, 1978
- Structural Determination of Three Glycoasparagines Isolated from the Urine of a Patient with AspartylglycosaminuriaEuropean Journal of Biochemistry, 1976
- Enzymatic Diagnosis and Carrier Detection of Aspartylglucosaminuria Using Blood SamplesPediatric Research, 1976
- Glycoasparagine metabolites in patients with aspartylglycosaminuria: comparison between english and finnish patients with special reference to storage materialsClinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Aspartylglucosaminuria: Deficiency of aspartylglucosaminidase in cultured fibroblasts of patients and their heterozygous parentsClinical Genetics, 1973
- ELEVEN NEW CASES OF ASPARTYLGLUCOSAMINURIA*Journal of Intellectual Disability Research, 1970
- ASPARTYLGLYCOSAMINURIAThe Lancet, 1968